Liu Jing, Pu Yi-Yi, Xie Qian, Wang Jia-Kun, Liu Jian-Xin
MoE Key Laboratory of Molecular Animal Nutrition, Institute of Dairy Science, College of Animal Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
Curr Microbiol. 2015 Jan;70(1):67-74. doi: 10.1007/s00284-014-0672-y. Epub 2014 Sep 2.
Pectin is a non-fiber carbohydrate (NFC) that exists in forages, but it is not clear how pectin exerts its effect on populations of either known microbial species or uncultured ruminal bacteria. PCR-denaturing gradient gel electrophoresis (PCR-DGGE) and real-time PCR analysis were used in the present study to investigate the effects of pectin on microbial communities in an in vitro rumen fermentation system. The fermentations were conducted using forage (corn stover or alfalfa), an NFC source (pectin or corn starch), or their combination as the substrates. Addition of pectin increased acetate (P < 0.05), whereas inclusion of starch increased butyrate production (P < 0.05). The pectate lyase activity was higher with alfalfa than with corn straw, or with pectin than with corn starch (P < 0.05), while the amylase activity was higher in corn starch-included treatments than the others (P < 0.05). The cluster analysis of the bacterial 16S rRNA gene showed that the DGGE banding patterns differed significantly between the treatments and led to the identification of three groups that were highly associated with the NFC sources. The specific bands associated with pectin-rich treatments were identified to be dominated by members of the Treponema genus. The growth of the Treponema genus was remarkably supported by the inclusion of pectin, highlighting their specific ability to degrade pectin. The results from the present study expand our knowledge of the microbial populations associated with pectin digestion, which may not only facilitate future research on utilization of pectin in feeds, but also improve our understanding of pectin digestion with respect to the rumen micro-ecosystem.
果胶是一种存在于草料中的非纤维碳水化合物(NFC),但目前尚不清楚果胶如何对已知微生物物种或未培养的瘤胃细菌群体产生影响。本研究采用聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)和实时荧光定量PCR分析,研究果胶对体外瘤胃发酵系统中微生物群落的影响。发酵实验以草料(玉米秸秆或苜蓿)、NFC源(果胶或玉米淀粉)或它们的组合作为底物进行。添加果胶可增加乙酸盐含量(P<0.05),而添加淀粉可提高丁酸盐产量(P<0.05)。苜蓿组的果胶酸裂解酶活性高于玉米秸秆组,果胶组高于玉米淀粉组(P<0.05),而含玉米淀粉处理组的淀粉酶活性高于其他处理组(P<0.05)。细菌16S rRNA基因的聚类分析表明,各处理间的DGGE条带模式存在显著差异,鉴定出与NFC源高度相关的三个组。与富含果胶处理相关的特定条带被鉴定为以密螺旋体属成员为主。添加果胶显著促进了密螺旋体属的生长,突出了它们降解果胶的特殊能力。本研究结果扩展了我们对与果胶消化相关微生物种群的认识,这不仅有助于未来饲料中果胶利用的研究,也有助于我们更好地理解瘤胃微生态系统中的果胶消化。